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rs6709476

From SNPedia

Orientationplus
Stabilizedplus
Make rs6709476(A;A)
Make rs6709476(A;G)
Make rs6709476(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position85216801
GeneLOC102724579, TCF7L1
is asnp
is mentioned by
dbSNPrs6709476
ebirs6709476
HLIrs6709476
Exacrs6709476
Varsomers6709476
Maprs6709476
PheGenIrs6709476
hapmaprs6709476
1000 genomesrs6709476
hgdprs6709476
ensemblrs6709476
gopubmedrs6709476
geneviewrs6709476
scholarrs6709476
googlers6709476
pharmgkbrs6709476
gwascentralrs6709476
openSNPrs6709476
23andMers6709476
23andMe allrs6709476
SNP Nexus

SNPshotrs6709476
SNPdbers6709476
MSV3drs6709476
GWAS Ctlgrs6709476
GMAF0.2466
Max Magnitude
? (A;A) (A;G) (G;G) 28


GET Evidence
rs6709476
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.289062
summary